Expandable absorbable implants have been developed that are suitable for breast reconstruction following mastectomy. The implants can be implanted in the vicinity of a tissue expander, for example, by suturing to the detached edge of the pectoralis major muscle to function as a pectoralis extender, and used to form a sling for a tissue expander. The implants, which permit tissue-ingrowth and slowly degrade, can be expanded in the breast using a tissue expander in order to form a pocket for a permanent breast implant. After expansion, the tissue expander can be removed and replaced with a permanent breast implant. The expandable implants help reduce patient discomfort resulting from tissue expansion, and avoid the need to use allografts or xenografts to create the pocket for the tissue expander. The expandable absorbable implant preferably comprises poly-4-hydroxybutyrate or copolymer thereof.

An accommodative intraocular lens includes an optic body having an optical power changing structure. There are two supporting structures disposed opposite one another about the optic body, each supporting structure configured to be connected at a distal end to a ciliary body after implantation in an eye of a patient and connected at a proximal end to the optic body. The two supporting structures are a zeroing supporting structure and an actuating supporting structure. The zeroing supporting structure is configured to not change the optical power of the optic body in an installation mode and an operation mode of the accommodative intraocular lens. An actuating supporting structure is configured to not change the optical power of the optic body in the installation mode but is configured to change the optical power of the optic body in the operation mode of the accommodative intraocular lens.

A penile prosthesis includes a penile prosthetic; a pump; a reservoir; first tubing adapted to couple the penile prosthetic to the pump; second tubing adapted to couple the reservoir to the pump; and a plate adapted to couple with the penile prosthetic. The plate is implantable and adapted to orient the penile prosthetic in an anatomically natal penis position that is adapted for penetrative intercourse.

Ophthalmic devices and ophthalmic systems including alignment sidewalls and blend zones disposed therethrough are described. An example ophthalmic device may include a first and a second optical element having alignment sidewalls shaped to cooperatively couple. The alignment sidewall may include blend zones disposed in the sidewall shaped to transition the sidewall from a ridge to a surface of an optic zone of the optical element. The alignment sidewalls may define a cavity disposed between two coupled optical elements when the alignment sidewalls are cooperatively coupled into which a liquid crystal may be disposed. A method of assembling an ophthalmic device is described. An example method may include aligning a blend zone of a first optical element with a mating blend zone of a second optical element. The example method may further include cooperatively coupling alignment sidewalls of the first optical element and the second optical element.

Embodiments of the application provide methods and systems for treating rotator cuff injuries including but not limited to a trilobe inflatable implant that may be rolled and even inflated. An implant placement tool with a filler to assist in implanting and filling a trilobe implant. A trilobe implant may be held in place with a parts of a shoulder area or may even be secured with a securement.

One or more sensors are incorporated onto one or more of an implantable device and a surgical tool used for placement and/or adjustment of the implantable device. The implantable device includes an adjustable membrane element for controllable coaptation of a body lumen, such as coaptation of a urethra as treatment for urinary incontinence. In various embodiments, the one or more sensors can be configured to detect information indicative of at least one of a shape of the adjustable membrane element, a position of the adjustable membrane element relative to the body lumen, or a shape of the body lumen.

The present invention relates to an integrated radial silicone-filled cell-structured for human body implant and manufacturing method thereof, and more particularly, in a human body implant, to an integrated radial silicone-filled cell-structured human body implant comprising: a first silicone-filled cell including a silicone filling material, in which the silicone filling material is formed in the center of the implant; and a second silicone-filled cell surrounding an outer surface of the first silicone-filled cell, being formed radially around the center of the implant, and including a silicone filling material formed with a cross-linking density different from a silicone cross-linking density of the first silicone-filled cell.

This invention addresses the need of repairing aortic aneurysms. The method embodies the manufacturing of patient and anatomy specific endovascular implant. Additional advantages of the invention relate to smaller delivery size, improving the risk of graft migration and endoleak formation.

Devices are disclosed for use in the transcatheter treatment of mitral valve regurgitation, specifically a coaptation assistance element for implantation across the mitral valve and an edge to edge device. Methods are disclose for reducing mitral valve regurgitation at low left ventricle pressure and high left ventricle pressure during the cardiac cycle. Devices are disclosed for use in the transcatheter treatment of mitral valve regurgitation, specifically a coaptation assistance element for implantation across the mitral valve with an adaptive coaptation element.

An apparatus for delivery of a device into a hollow organ and a method of delivery are provided. The apparatus includes an elongated tube having proximal and distal openings and being configured for carrying the device on a distal portion thereof. The apparatus further includes a tubular cover for covering at least a portion of the device when mounted on the elongated tube, the tubular cover being radially elastic and axially non-elastic. The tubular cover is retrievable into the elongated tube through the distal opening, such that when the device is mounted on the elongated tube and covered by the tubular cover, retrieval of the tubular cover into the elongated tube uncovers the device for delivery into the hollow organ.